1. A 40-year old female presented with a proliferative mass in the right parotid gland and duct. Surgical excision was performed and histopathological examination revealed the presence of Rhinosporidium seeberi, confirming a rare case of rhinosporidiosis involving the parotid duct. 2. Rhinosporidiosis is a benign fungal infection caused by Rhinosporidium seeberi, most commonly involving the nose and nasopharynx. Primary involvement of the parotid duct is extremely rare. 3. Diagnosis is made through histopathological identification of the characteristic sporangia of R. seeberi. Treatment involves surgical resection as recurrence

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Middle East
Journal of
Case Reports
Middle East Journal of Case Reports 2016; 1: 1–3
http://scigatejournals.com/publications/index.php/mejcr
Page | 1
Rhinosporidiosis of Parotid Duct
A K M Maruf Raza1
*, Ajoy Bordhon2
, Popy Roy3
1. Assistant Professor, Department of Pathology, Jahurul Islam Medical College, Kishoregonj, Bangladesh.
2. Associate Professor, Department of otolaryngology, Jahurul Islam medical College, Kishoregonj, Bangladesh.
3. Assistant Professor, Department of Pharmacology, Jahurul Islam Medical College, Kishoregonj, Bangladesh.
Abstract
Rhinosporidiosis is a benign chronic granulomatous fungal infection caused by Rhinosporidium seeberi (R. seeberi), Rhinosporid-
ium kinealyi (R. kinealy). Rhinosporidiosis is endemic in South Asia, notably in Southern India and Sri Lanka.The common sites
of involvement are the nose and nasopharynx followed by ocular tissue. Rhinosporidiosis is also known to involve many rare sites
and may become disseminated to ocular in generalized form. Rhinosporidiosis of parotid duct is extremely rare. The case presented
here is of a 40 years old female from a village of Bajitpur, Kishoregonj with proliferative mass in the right parotid gland and parotid
duct. Surgical excision was done and the specimen was sent for histopathological examination. Although rhinosporidiosis was not
taken into consideration in the clinical differential diagnosis, eventual histopathological diagnosis confirmed rhinosporidiosis.
Key words: Parotid duct, Rhinosporidiosis, Histopathology, Granulomatous infection
Citation to This Article: Maruf Raza AKM, Bordhon A, Roy P. Rhinosporidiosis of Parotid Duct. Middle East Journal of Case Reports 2016; 1:
1–3.
1. Introduction
Rhinosporidiosis is a benign chronic granulomatous fungal disease caused by Rhinosporidium seeberi (R. seeberi) (1).
It occurs sporadically and is known to be noncontagious. Although human rhinosporidiosis occurs universally with
higher occurrence in parts of South Asia, it is endemic, especially in Southern India and Sri Lanka (2). The most
common site of infection in humans is the nose. Other sites include the nasopharynx, larynx, oropharynx, conjunctiva,
lacrimal sac, and genital mucosa. Intraorally, rhinosporidiosis is known to involve the lip, palate, and uvula, second-
arily, by direct extension from nasal and nasopharyngeal lesions1
. Primary involvement of the parotid duct is extremely
rare. We present a case of 40-year-old female from a village of Bhagalpur, Kishoregonj with proliferative mass in the
right parotid gland and parotid duct. Surgical excision was done and the presence of R. seeberi on histopathologic
analysis of the specimen was seen.
2. Case Report
A 40-year-old female reported to the department of otolaryngology with complaints of swelling on right side of the
face since 5 months, associated with a history of an increase in its size and also pain associated with swelling. No
other associated symptoms were reported. There was no history of trauma in the recent past. Patient had history of
consumption of unprocessed well water. On clinical examination, patient was moderately built with no signs of parlor,
jaundice, or lymphadenopathy. Systemic examination also did not reveal any abnormalities. The nose, nasopharynx,
oropharynx, and eyes appeared normal. On local examination, there was a single, soft to firm consistency, discrete
swelling on the right side of the cheek measuring about 4 × 3cm. Overlying skin was normal in color and texture with
* Corresponding author: Dr. A. K. M. Maruf Raza
Tel: +8801711306123
E-mail address: drmarufraza@gmail.com

2. Maruf Raza A.K.M. et al. Middle East Journal of Case Reports 2016; 1: 1–3
Page | 2
no local rise of temperature. There was tenderness felt on palpation with no fixity to underlying skin or structure.
Routine laboratory investigation revealed eosinophilia (eosinophils,15%). The fine needle aspiration cytology
(FNAC) showed presence of neutrophils and lymphocytes admixed with clusters and acini of ductal and myoepithelial
cells. Ultrasonography (USG) showed a solid and cystic lesion in the subcutaneous plane of cheek of size 3 × 1.6 cm,
with echogenic debris and internal septations. Surgical excision of the lesion was done under general anesthesia. The
lesion was identified as dilated segment of the parotid itself. The proximal and distal parts of the ducts were dissected
further and were found to be in continuity with the mass itself. The excised specimen was submitted for histopatho-
logic examination. The hematoxylin-eosin stained sections showed thin fibrocollagenous cystic wall lined by colum-
nar to cuboidal to flattened cells. One of the parts of the specimen showed the presence of numerous, sporangia of R.
seeberi (Figure 1 and 2). Histopathological examination confirmed the diagnosis of rhinosporidiosis of the parotid
gland duct.
3. Discussion
The pathogen R. seeberi was first discovered by Malbran in 1892 and later, cases in cattle were reported in India in
1894 (3). It was first described by Seeber (4) in 1900 in the nasal region in his doctoral thesis of medicine. Review of
the literature shows frequency of the disease to be greater in South Asia, with the largest number of cases having been
reported in Southern India and Sri Lanka (2). Men are affected more than women (male: female ratio, 4: 1). Patients
of all ages are affected, but the disease most frequently occurs in those aged between 20 and 35 years. Common sites
of involvement include the nose and upper respiratory tract (1). In our case the parotid was considered to be the
primary site of inoculation of the organism because there were no other nasal or nasopharyngeal lesions. The diagnosis
of rhinosporidiosis is primarily made by observing the distinctive morphologic features of R. seeberi in affected tissue.
Its life cycle begins in the tissue as a spore, and it passes through several stages of development from trophocyte to
juvenile sporangium to mature forms with changes in thickness and lamination of walls. Nuclear condensation takes
place to form endospores embedded in a mucoid matrix. Characteristically, special electron dense bodies of about 1
to 3mm are seen in mature endospores. These endospores become extruded into the surrounding thick sporangial wall
and eventually develop into trophocytes to perpetuate their life cycle (5).
The most common mode of spread to host is by transepithelial infection or by autoinoculation. Infection with R.
seeberi is most likely waterborne. A high incidence has been observed in patients who dive and swim in stagnant
water (6). Individuals probably acquire the disease from water contaminated by diseased cattle. As our case patient
had history of consumption of unprocessed well water. Because the organism has not been isolated in culture, the
histopathologic examination remains the gold standard for diagnosis (7). The larger and thick walled sporangia of R.
seeberi differentiate this lesion distinctly from the organism causing coccidioidomycosis (8). The only drug which has
been shown to have some rhinosporicidal effect is Dapsone, which arrests the maturation of sporangia and promotes
fibrosis in the stroma, when used as an adjunct to surgery (6). Treatment of choice is surgical resection (1), as most
recurrences occur due to spillage of endospores on adjacent mucosa.
4. Conclusion
Rhinosporidiosis is a benign chronic granulomatous fungal disease caused by Rhinosporidium seeberi (R. seeberi).
The most common site of infection in humans is the nose. Other sites include the nasopharynx, larynx, oropharynx,
conjunctiva, lacrimal sac, and genital mucosa. Primary involvement of the parotid duct is extremely rare. We present
a case of 40-year-old female from a village of Bhagalpur, Kishoregonj with proliferative mass in the right parotid
gland and parotid duct. The purpose of this report is to encourage clinicians to be flexible in the differential diagnosis
of proliferative growth in the parotid duct, even in those from nonendemic areas.
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